| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | Autosomal recessive juvenile Parkinson disease 2 +4 more | |
| | | Single nucleotide variant (missense variant) | Autosomal recessive juvenile Parkinson disease 2 +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | LOC126859871, PRKN (S167N) | Single nucleotide variant (missense variant +1 more) | not provided +4 more | |
Click to view in NCBI Gene